Pomalidomid Viatris
The medicinal product has been authorised by the European Commission (EC) via centralised procedure in all EU Member States, based on the European Medicines Agency (EMA) experts' opinion.
Name | Pomalidomid Viatris |
---|---|
Active Substance | pomalidomid |
Prescription | na recept |
Type of prescription | ograničeni recept |
Distribution | u ljekarni |
ATC Code | L04AX06 |
Summary of product characteristics (SmPC), labelling and package leaflet (PL) | download |
Link to the European Medicines Agency's (EMA) product information | download |
Link to the European Commission's (EC) decisions | download |
Educational materials for healthcare professionals |
Vodič za zdravstvene radnike, verzija 5 Obrazac svjesnosti o rizicima, verzija 1 Obrazac za praćenje trudnoće, verzija 4 |
Educational materials for patients / caregivers |
Vodič za bolesnike, verzija 5 Kartica za bolesnika, verzija 4 |